Canonical Allele Identifier: CA2189568069
Gene: HYKK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534633G= , CM000677.2:g.78534633G= GRCh38
NC_000015.9:g.78826975G= , CM000677.1:g.78826975G= GRCh37
NC_000015.8:g.76614030G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388988.9:c.*963G= MANE Select ENSP00000373640.4:n.*963G=
ENST00000408962.6:c.662-2667G= ENSP00000386197.2:n.662-2667G=
ENST00000563233.2:c.662-2667G= ENSP00000454850.1:n.662-2667G=
ENST00000569878.5:c.2085G= ENSP00000455459.1:n.2085G=
NM_001083612.1:c.662-2667G= NP_001077081.1:n.662-2667G=
NM_001013619.3:c.*963G= NP_001013641.2:n.*963G=
NM_001013619.4:c.*963G= MANE Select NP_001013641.2:n.*963G=
NM_001083612.2:c.662-2667G= NP_001077081.1:n.662-2667G=
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